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庚醇对豚鼠输精管神经源性和肌源性收缩的影响。

Effects of heptanol on the neurogenic and myogenic contractions of the guinea-pig vas deferens.

作者信息

Venkateswarlu K, Dange S Y, Manchanda R

机构信息

School of Biomedical Engineering, Indian Institute of Technology, Powai, Mumbai.

出版信息

Br J Pharmacol. 1999 Jan;126(1):227-34. doi: 10.1038/sj.bjp.0702307.

Abstract
  1. The effects of the putative gap junction uncoupler, 1-heptanol, on the neurogenic and myogenic contractile responses of guinea-pig vas deferens were studied in vitro. 2. Superfusion of 2.0 mM heptanol for 20-30 min produced the following reversible changes in the biphasic neurogenic contractile response (8 trials): (i) suppression of both phases; (ii) delayed development of both the first as well as the second phase, accompanied by complete temporal separation of the two phases; (iii) prominent oscillations of force during the second (noradrenergic) phase only. 3. To eliminate prejunctional effects of heptanol, myogenic contractions were evoked by field stimulation of the vas in the presence of suramin (200 microM) and prazosin (1 microM). Heptanol (2.0 mM) abolished these contractions reversibly. 4. These results show that (i) heptanol inhibits both excitatory junction potential (EJP)-dependent and non EJP-dependent contractions of the vas; (ii) a postjunctional site of action of heptanol, probably intercellular uncoupling of smooth muscle cells, contributes to the inhibition of contraction.
摘要
  1. 研究了假定的缝隙连接解偶联剂1-庚醇对豚鼠输精管神经源性和肌源性收缩反应的体外作用。2. 用2.0 mM庚醇灌注20 - 30分钟,在双相神经源性收缩反应中产生了以下可逆变化(8次试验):(i)两个阶段均受抑制;(ii)第一阶段和第二阶段的发展均延迟,且两个阶段在时间上完全分离;(iii)仅在第二(去甲肾上腺素能)阶段出现明显的力量振荡。3. 为消除庚醇的节前效应,在苏拉明(200 microM)和哌唑嗪(1 microM)存在的情况下,通过对输精管进行场刺激诱发肌源性收缩。庚醇(2.0 mM)可使这些收缩可逆地消失。4. 这些结果表明:(i)庚醇抑制输精管中依赖兴奋性接头电位(EJP)和不依赖EJP的收缩;(ii)庚醇的节后作用位点,可能是平滑肌细胞间的解偶联,有助于抑制收缩。

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